Role of sphingolipids in the pathogenesis of intrahepatic cholestasis
•Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory distress syndrome and intrauterine fetal demise.•Cholestasis treatment with UDCA is known to be very effective.•Sphingolipids can potentially becom...
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Published in | Prostaglandins & other lipid mediators Vol. 147; p. 106399 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.04.2020
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Abstract | •Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory distress syndrome and intrauterine fetal demise.•Cholestasis treatment with UDCA is known to be very effective.•Sphingolipids can potentially become screening markers as well as markers for monitoring the treatment of ICP in pregnant women.
Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms.
Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay – before the commencement of treatment with ursodeoxycholic acid (UDCA) – and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls.
Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline.
It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy. |
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AbstractList | Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms.
Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay - before the commencement of treatment with ursodeoxycholic acid (UDCA) - and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls.
Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline.
It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy. Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms.BACKGROUND & AIMSIntrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms.Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay - before the commencement of treatment with ursodeoxycholic acid (UDCA) - and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls.METHODSTwenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay - before the commencement of treatment with ursodeoxycholic acid (UDCA) - and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls.Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline.RESULTSOf all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline.It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy.CONCLUSIONIt is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy. •Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory distress syndrome and intrauterine fetal demise.•Cholestasis treatment with UDCA is known to be very effective.•Sphingolipids can potentially become screening markers as well as markers for monitoring the treatment of ICP in pregnant women. Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is connected with increased risk of fetal morbidity and mortality, but is unfortunately detected quite late. The diagnosis of ICP is based on only one manifestation: pruritus which mainly affects soles and palms. Twenty intrahepatic cholestasis of pregnancy (ICP) women and twenty healthy pregnant women (control group) took part in the study. In the study group, blood sampling for baseline measurements was performed on the first day of hospital stay – before the commencement of treatment with ursodeoxycholic acid (UDCA) – and repeated after 7 days of 900 mg UDCA per day. An additional blood sample was collected on the second day after childbirth. In the control group, blood samples were collected directly after hospital admission. We compared plasma sphingolipids in samples of the subjects from ICP and ICP + UDCA-treated groups as well as the ICP group after delivery with the healthy controls. Of all sphingolipids, the median values of C16-Cer and C18-Cer were significantly higher in the plasma of cholestasis patients not treated with UDCA as compared to the control. Following 7 days of UDCA treatment, a considerable decrease in C16-Cer, C18-Cer and the total concentration of bile acids was noted as compared to the baseline. It is known that sphingolipids serve as modulators of liver regeneration. We assume these substances could be potential markers for detecting early onsets of intrahepatic cholestasis of pregnancy. |
ArticleNumber | 106399 |
Author | Kacerovsky, Marian Blachnio-Zabielska, Agnieszka Kosinski, Przemyslaw Mikucka-Niczyporuk, Agnieszka Charkiewicz, Karol Laudanski, Piotr Knas, Małgorzata Pierzynski, Piotr Lemancewicz, Adam |
Author_xml | – sequence: 1 givenname: Agnieszka surname: Mikucka-Niczyporuk fullname: Mikucka-Niczyporuk, Agnieszka organization: Department of Perinatology, Medical University of Bialystok, Poland – sequence: 2 givenname: Piotr surname: Pierzynski fullname: Pierzynski, Piotr organization: Department of Perinatology, Medical University of Bialystok, Poland – sequence: 3 givenname: Adam surname: Lemancewicz fullname: Lemancewicz, Adam organization: Department of Perinatology, Medical University of Bialystok, Poland – sequence: 4 givenname: Przemyslaw orcidid: 0000-0003-3812-7560 surname: Kosinski fullname: Kosinski, Przemyslaw email: pkosinski@wum.edu.pl organization: 1st Department of Obstetrics and Gynecology, Medical University of Warsaw, Poland – sequence: 5 givenname: Karol surname: Charkiewicz fullname: Charkiewicz, Karol organization: Department of Perinatology, Medical University of Bialystok, Poland – sequence: 6 givenname: Małgorzata surname: Knas fullname: Knas, Małgorzata organization: Department of Cosmetology, Lomza State University of Applied Sciences, Poland – sequence: 7 givenname: Marian surname: Kacerovsky fullname: Kacerovsky, Marian organization: Department of Obstetrics and Gynecology, University Hospital Hradec Kralove, Charles University, Faculty of Medicine in Hradec Kralove, Czech Republic – sequence: 8 givenname: Agnieszka orcidid: 0000-0002-8055-0576 surname: Blachnio-Zabielska fullname: Blachnio-Zabielska, Agnieszka organization: Department of Hygiene, Epidemiology and Metabolic Disorders, Medical University of Bialystok, Poland – sequence: 9 givenname: Piotr surname: Laudanski fullname: Laudanski, Piotr organization: 1st Department of Obstetrics and Gynecology, Medical University of Warsaw, Poland |
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Keywords | liver disorder Sphingolipids cholestasis ceramides |
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Snippet | •Intrahepatic cholestasis related perinatal complications include premature birth, meconium-stained amniotic fluid, fetal bradycardia, fetal respiratory... Intrahepatic cholestasis of pregnancy (ICP) is the most common pregnancy-related liver disorder that affects from 0.2% to 15.6% pregnant women. The disease is... |
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SubjectTerms | Adult Bile Acids and Salts - blood Biomarkers - blood Case-Control Studies ceramides Cholagogues and Choleretics - therapeutic use cholestasis Cholestasis, Intrahepatic - blood Cholestasis, Intrahepatic - drug therapy Cholestasis, Intrahepatic - pathology Female Fetus - abnormalities Humans liver disorder Pregnancy Pregnancy Complications - blood Pregnancy Complications - drug therapy Pregnancy Complications - pathology Sphingolipids Sphingolipids - blood Ursodeoxycholic Acid - therapeutic use |
Title | Role of sphingolipids in the pathogenesis of intrahepatic cholestasis |
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